Mölnlycke® Static Air Boots

GUDID 07323190260607

Pediatric Heel Protector

Mölnlycke Health Care AB

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• Primary Device ID: 07323190260607
• NIH Device Record Key: d42133a9-2f8a-497d-8941-6777024d18c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mölnlycke® Static Air Boots
• Version Model Number: 1400111
• Company DUNS: 631770658
• Company Name: Mölnlycke Health Care AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07323190260607 [Primary]

FDA Product Code

• FMP: Protector, skin pressure

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-03-16
• Device Publish Date: 2022-12-13

Devices Manufactured by Mölnlycke Health Care AB

• 07333350122089 - Mepilex® Border Post-Op: 2024-07-08 Mepilex Border Post Op 10x30cm
• 07333350293765 - Mepilex® Up: 2024-06-26 Mepilex Up 5x5cm
• 07333350888848 - Mepilex® Up: 2024-06-26 Mepilex Up 20x50cm
• 07333350376345 - Mepilex® Border Post-Op: 2024-06-25 Mepilex Border Post Op 10x35cm
• 07333350078133 - Mepilex® Border Post-Op: 2024-06-25 Mepilex Border Post Op 9x10cm
• 07333350312497 - Mepilex® Border Post-Op: 2024-06-25 Mepilex Border Post-Op 6x8cm
• 07333350949082 - Mepilex® Border Post-Op: 2024-06-25 Mepilex Border Post Op 10x15cm
• 07333350710545 - Mölnlycke®: 2024-04-01 CAP FLORY